Position: Clinical Quality Associate

vor 2 Wochen

Berlin, Deutschland Meditrial Europe Ltd. Vollzeit

Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals.

Since 2008, Meditrial delivers unparalleled outcomes for innovators. Our successful track record supporting the lifescience industry manufacturers in all phases of clinical development puts us in a prime position to seize the opportunity to emerge as a leader in digital technology with the promise that it will enhance and alleviate the clinical trial and participant burden. Through our work, the patient and innovator are empowered with data and insights across the lifecycle of product development and market penetration changing the paradigm of care towards understanding and value. We have the ability to transcend the current landscape with “smart” technology enabled data collection tools and insights.

Meditrial offers highest level expertise across multiple therapeutic areas. We are passionate about our mission to support the innovation and development of better therapies in compliance with solid ethical standards. Our commitment has resulted in excellent results for business growth by creating stability and opportunities for employees and collaborators.

**Position: Clinical Quality Associate**:
**Industry**: Lifescience Industry: Pharma, Medtech, Digital Health

**Employment Type**: Full-time

**Job Functions**: Clinical Affairs

**Location**: Meditrial GmbH, Kantstrasse 21, 10623, Berlin, Germany

**Workplace**: In Office

The Clinical Quality Associate provides support to all organizational levels to operate in compliance with international regulations in every aspect of clinical development and clinical trial conduct. The ideal profile would be practical-minded and should have lifesciences and quality expertise and a background in clinical operations.

**Responsibilities**:

- Assist Clinical Quality Manager with various administrative tasks
- Support the clinical team for the management of clinical trials including the EDC System and CTMS as defined by the Quality System Procedures (SOPs);
- Support the clinical project team in the assessment and management of clinical trials with medical devices (mainly cardiovascular therapeutic area) according to current regulations;
- Collect, review, draft and track regulatory and investigator documents as required for the submission to the Competent Authorities and Ethics Committee; maintaining, updating and filing documents;
- Perform administrative tasks required during study start-up activities (e.g. word processing, collecting study documents, relation management with Study Investigators, updating internal progress reports);
- SAE Notification to Competent Authorities and Ethics Committee.
- Provide support for creation and maintenance of reports, charts, spreadsheets, documents and presentations;
- Establish, maintain and update files and records as needed;
Skillset & Qualifications
- Education: Bachelor’s degree, Master is a plus;
- Minimum 2 years experience in life science field and Quality Management;
- Languages: proficiency in oral and written English and German (a third language considered a plus);
- Proficient in Microsoft Office (MS Outlook, MS Word, MS Excel, Ms Power Point);

  • Clinical Trial Associate

    vor 4 Wochen

    Berlin, Deutschland Elixir Associates Vollzeit

    Company: Elixir Associates are currently partnering with a rapidly growing European biotech developing next-generation therapies in the critical-care / cardiology space. The company is expanding its Clinical Operations team and seeking a talented Clinical Trial Associate to support their advancing clinical programs across multiple Phase 2 studies. About The...

  • Clinical Trial Associate

    vor 4 Wochen

    Berlin, Deutschland Elixir Associates Vollzeit

    Company:Elixir Associates are currently partnering with a rapidly growing European biotech developing next-generation therapies in the critical-care / cardiology space. The company is expanding its Clinical Operations team and seeking a talented Clinical Trial Associate to support their advancing clinical programs across multiple Phase 2 studies.About The...

  • Clinical Research Lead

    vor 2 Wochen

    Berlin, Deutschland Advanced Clinical Vollzeit

    The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, to support client';s pipeline, in accordance with ICH/GCP, client SOPs, local operating guidelines and local requirements, as applicable. CRL works locally, supporting Associate Director Clinical Operations (ADCO) /...

  • Clinical Research Associate

    vor 2 Wochen

    Berlin Metropolitan Area, Deutschland SCIRENT Clinical Research and Science Vollzeit

    SCIRENT Clinical Research and Science is seeking a motivated Clinical Research Associate for a full-time position in Germany, ideally based in Berlin or willing to relocate to Berlin. Candidates must be fluent in English and German. Proficiency in an additional language (Greek, Italian, or a Scandinavian language) would be advantageous.___Area of...

  • Clinical Trial Associate

    vor 4 Wochen

    Berlin, Deutschland Elixir Associates Vollzeit

    Elixir Associates are currently partnering with a rapidly growing European biotech developing next-generation therapies in the critical-care / cardiology space. The company is expanding its Clinical Operations team and seeking a talented Clinical Trial Associate to support their advancing clinical programs across multiple Phase 2 studies. Reporting...

  • Clinical Research Associate

    Vor 4 Tagen

    Berlin, Deutschland Antal Sp. z o.o. Vollzeit

    Clinical Research Associate (CRA) Location: Germany (Remote )   Job Description:We are seeking a highly motivated  Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with...

  • Clinical Project Manager

    vor 3 Wochen

    Berlin, Deutschland SCIRENT Clinical Research and Science Vollzeit

    SCIRENT Clinical Research and Science is seeking a dedicated Clinical Project Manager for a full-time position in Germany. As a Clinical Project Manager, you will be responsible for the planning, coordination, and execution of clinical trials in the cardiovascular field. You will be the primary point of contact for internal teams, external partners, and...

  • Position: Head of Clinical Operations

    vor 2 Wochen

    Berlin, Deutschland Meditrial Europe Ltd. Vollzeit

    Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

  • Clinical Operations Associate

    vor 1 Woche

    Berlin, Berlin, Deutschland Eucalyptus Vollzeit

    About EucalyptusAtEucalyptus (EUC), we're on a mission to make good health last a lifetime. More than one billion people globally live with obesity a leading cause of preventable chronic diseases like diabetes and heart disease.ThroughJuniper, our flagship weight-management brand, we combineGLP-1 medicationwith personalised nutrition, exercise, and ongoing...

  • Clinical Trial Ambassador

    vor 2 Wochen

    Berlin, Deutschland Syneos Health Clinical Vollzeit

    **Overview** The Clinical Trial Ambassador will establish, cultivate, and maintain scientific relationships with investigators and study coordinators to support enrollment while developing a strong understanding of clinical practice as it relates to areas of interest. This position interacts with various internal and external stakeholders, with a focus on...